2,2,2-Trifluoroethanol → 5-Bromo-6-(2,2,2-trifluoro-ethoxy)-pyridine-2-carboxylic acid

HRID 632341

반응식

HRID 632341 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:9]([OH:11])=[O:10])=[N:6][C:7]=1Cl.[OH-].[K+].[F:14][C:15]([F:19])([F:18])[CH2:16][OH:17]>CS(C)=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:9]([OH:11])=[O:10])=[N:6][C:7]=1[O:17][CH2:16][C:15]([F:19])([F:18])[F:14]

참가 물질

5

실험 절차

In a 25 mL round-bottomed flask, 5-bromo-6-chloropicolinic acid (433 mg, 1.83 mmol) and powdered potassium hydroxide (411 mg, 7.32 mmol) were combined with DMSO (1.9 ml) to give a colorless solution which was stirred at room temperature for 15 min. 2,2,2-trifluoroethanol (275 mg, 198 μl, 2.75 mmol, Eq: 1.5) was added. The reaction mixture was stirred for 24 h at ambient temperature. Since the reaction was complete, 0.75 extra equivalents of 2,2,2-trifluoroethanol was added and the reaction was stirred 48 h at ambient temperature. The reaction mixture was poured onto 1 M HCl/ice water (1×20 mL), extracted with iPrOAc (2×25 mL). The organic layers were dried over Na2SO4 and filtered, removed under reduced pressure to give the title compound as a white solid after recrystallization from CH2Cl2 and heptane (409 mg, 1.36 mmol, 74.4% yield), MS (EI): m/e=299.9 [M+H]+.

후처리

  1. customto give a colorless solution which
  2. stirringThe reaction mixture was stirred for 24 h at ambient temperature
  3. stirringthe reaction was stirred 48 h at ambient temperature
  4. extractionextracted with iPrOAc (2×25 mL)
  5. dry with materialThe organic layers were dried over Na2SO4
  6. filtrationfiltered
  7. customremoved under reduced pressure

출처 및 근거

ORD 기록
ord-435769ce8386413398184ccdfee05eff
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09321727B2

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